Content
Regulatory requirements are increasing across industries. Especially for Medical Devices incomplete submissions and lack of cohesive structure of technical documentation are the most common reasons for market approval delays, according to Notified Bodies. This presentation will explore how a data-driven approach to content management can ensure consistency across data and content and avoid delays in documentation reviews and device registrations.
Takeaways
Participants will learn techniques of working more closely with product data to make content creation and delivery more compliant and accurate, and to make content an ever more valuable asset for its users, to reach their specific goals.
Prior knowledge
Basic Knowledge of CCMS and typical technical documentation processes